FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CoaguChek XS Plus System

K Number: K253188 · Decision Oct 24, 2025
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
183
Review Days
28

Basic Information

Device Name
CoaguChek XS Plus System
K Number
K253188
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Roche Diagnostics
Date Received
September 26, 2025
Decision Date
October 24, 2025
Product Code
GJS
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GJS Test, Time, Prothrombin

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